Submitter | Handle | PJP | Submitter SNP ID | DIP_126429_chr11_10541070 | RefSNP(rs#) | rs71034774 | Submitted Batch ID | NSMB2011_INDEL | Submitted Date | Jan 21, 2011 | Publication Cited | [1] Impact of chromatin structure on sequence variability in the human genome | First entry to dbSNP | Jan 21 2011 12:00:00:000AM |
| Resource Links | Submitted Gene Name | N.D | Submitted Gene ID | N.D. | Submitted SNP Synonyms | N.D | Submitted linkout | N.D |
| Assay | Species | Homo sapiens | Molecular Type | Genomic | Method | TRACESALIGNMENT | Ascertainment Samplesize | N.D. | Population | N.D. |
| Allele | Observed Allele | -/T | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | DIV | CpG Code | N.D. |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss294688725|allelePos=52|len=103|taxid=9606|alleles='-/T'|mol=Genomic CAGTAATGAG ACGTTAGACA AATGTGTTTA CATCCTTTGA ACTCGGTTTC T
N
TTTTTTTTTT TTTTTTTTTT TTTTGAGACG GAGTCTCACT CTGTCGCCCA G
There is no frequency submission for ss294688725.
No sufficient data to compute Hardy-weinberg probability for ss294688725.
There is no individual genotype data for ss294688725.
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